| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:50244484-50244637 | Common:1; Rare:48 | ||||
| chr22:50244954-50245059 | Common:2; Rare:40 | ||||
| chr22:50280955-50281150 | Rare:74 | ||||
| chr22:50282269-50282409 | Common:2; Rare:41 | ||||
| chr22:50286077-50286235 | Common:1; Rare:50 | ||||
| chr22:50525524-50525716 | Common:4; Rare:94; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:50562887-50563091 | Common:3; Rare:52 | ||||
| chr22:50582385-50582449 | Rare:32 | ||||
| chr22:50582784-50583176 | Common:9; Rare:138; Clinvar:2; Clinvar (benign):3 | ||||
| chr22:50628073-50628276 | Common:9; Rare:97; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50783574-50783859 | Common:2; Rare:95 | ||||
| chr3:196982-197324 | Common:3; Rare:125 | ||||
| chr3:2098603-2098962 | Common:4; Rare:144 | ||||
| chr3:3126813-3126979 | Common:4; Rare:71; Clinvar (benign):1 | ||||
| chr3:4303253-4303648 | Common:3; Rare:149 |